A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3917242



Internal ID11497943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15267585..15267585hg38UCSC Ensembl
chrX:15285707..15285707hg19UCSC Ensembl
chrX:15195628..15195628hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38851
hg19851
hg18851
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1774504
Supporting Variants
SamplesHuRef
Known GenesASB9
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3917242
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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